BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 23729537)

  • 1. Early presentation of bilateral gonadoblastomas in a Denys-Drash syndrome patient: a cautionary tale for prophylactic gonadectomy.
    Patel PR; Pappas J; Arva NC; Franklin B; Brar PC
    J Pediatr Endocrinol Metab; 2013; 26(9-10):971-4. PubMed ID: 23729537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An unusual phenotype of Frasier syndrome due to IVS9 +4C>T mutation in the WT1 gene: predominantly male ambiguous genitalia and absence of gonadal dysgenesis.
    Melo KF; Martin RM; Costa EM; Carvalho FM; Jorge AA; Arnhold IJ; Mendonca BB
    J Clin Endocrinol Metab; 2002 Jun; 87(6):2500-5. PubMed ID: 12050205
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A review of the phenotypic variation due to the Denys-Drash syndrome-associated germline WT1 mutation R362X.
    Heathcott RW; Morison IM; Gubler MC; Corbett R; Reeve AE
    Hum Mutat; 2002 Apr; 19(4):462. PubMed ID: 11933209
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Case report: WT1 exon 6 truncation mutation and ambiguous genitalia in a patient with Denys-Drash syndrome.
    Chiang PW; Aliaga S; Travers S; Spector E; Tsai AC
    Curr Opin Pediatr; 2008 Feb; 20(1):103-6. PubMed ID: 18197048
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel WT1 heterozygous nonsense mutation (p.K248X) causing a mild and slightly progressive nephropathy in a 46,XY patient with Denys-Drash syndrome.
    da Silva TE; Nishi MY; Costa EM; Martin RM; Carvalho FM; Mendonca BB; Domenice S
    Pediatr Nephrol; 2011 Aug; 26(8):1311-5. PubMed ID: 21559934
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prophylactic bilateral salpingo-oopherectomy in a 17-year-old with Frasier syndrome reveals gonadoblastoma and seminoma: a case report.
    Love JD; DeMartini SD; Coppola CP
    J Pediatr Surg; 2006 Nov; 41(11):e1-4. PubMed ID: 17101338
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.
    Yue Z; Pei Y; Sun L; Huang W; Huang H; Hu B; Yang J; Jiang X; Mo Y; Chen S; Lai KN; Wang Y
    Ren Fail; 2011; 33(9):910-4. PubMed ID: 21851196
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome.
    Hakan N; Aydin M; Erdogan O; Cavusoglu YH; Aycan Z; Ozaltin F; Zenciroglu A; Apaydin S; Gunes R; Sahin G; Cinar G; Okumus N
    Genet Couns; 2012; 23(2):255-61. PubMed ID: 22876585
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defect.
    Cho HY; Lee BS; Kang CH; Kim WH; Ha IS; Cheong HI; Choi Y
    Pediatr Nephrol; 2006 Dec; 21(12):1909-12. PubMed ID: 16932893
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene.
    Furtado LV; Pysher T; Opitz J; Lamb R; Comstock J; Batish S; Mauch T; Nelson R; Zhou H
    Fetal Pediatr Pathol; 2011; 30(4):266-72. PubMed ID: 21434831
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical and pathological features of Denys-Drash syndrome: report of 3 cases].
    Wang HY; Sun LZ; Yue ZH; Yang J; Jiang XY; Mo Y
    Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):855-8. PubMed ID: 23302619
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Denys-Drash syndrome and gonadoblastoma in a patient with Klinefelter syndrome.
    Tanteles GA; Oakley S; Christian M; O'Neill D; Suri M
    Clin Dysmorphol; 2011 Jul; 20(3):131-135. PubMed ID: 21552011
    [No Abstract]   [Full Text] [Related]  

  • 13. A familial WT1 mutation associated with incomplete Denys-Drash syndrome.
    Zhu C; Zhao F; Zhang W; Wu H; Chen Y; Ding G; Zhang A; Huang S
    Eur J Pediatr; 2013 Oct; 172(10):1357-62. PubMed ID: 23715653
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prophylactic bilateral nephrectomy and preemptive kidney transplantation for Denys-Drash syndrome prior to development of kidney failure.
    Hosokawa C; Hotta K; Okamoto T; Cho Y; Hirose T; Iwahara N; Manabe A; Shinohara N
    Pediatr Nephrol; 2024 Mar; 39(3):905-909. PubMed ID: 37572117
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A case of Denys-Drash syndrome with prophylactic bilateral nephrectomy].
    Yamamoto K; Santo Y; Satomura K
    Nihon Jinzo Gakkai Shi; 2003; 45(1):42-6. PubMed ID: 12680320
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel WT1 mutation (C388Y) in a female child with Denys-Drash syndrome.
    Swiatecka-Urban A; Mokrzycki MH; Kaskel F; Da Silva F; Denamur E
    Pediatr Nephrol; 2001 Aug; 16(8):627-30. PubMed ID: 11519891
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Denys-Drash syndrome.
    Kucinskas L; Rudaitis S; Pundziene B; Just W
    Medicina (Kaunas); 2005; 41(2):132-4. PubMed ID: 15758579
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gonad development in Drash and Frasier syndromes depends on WT1 mutations.
    Jaubert F; Vasiliu V; Patey-Mariaud de Serre N; Auber F; Jeanpierre C; Gubler MC; Nihoul-Fékété C; Fellous M
    Arkh Patol; 2003; 65(2):40-4. PubMed ID: 15357247
    [TBL] [Abstract][Full Text] [Related]  

  • 19. WT1 gene mutation responsible for male sex reversal and renal failure: the Frasier syndrome.
    Saylam K; Simon P
    Eur J Obstet Gynecol Reprod Biol; 2003 Sep; 110(1):111-3. PubMed ID: 12932885
    [TBL] [Abstract][Full Text] [Related]  

  • 20. WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome.
    Guaragna MS; Ribeiro de Andrade JG; de Freitas Carli B; Belangero VM; Maciel-Guerra AT; Guerra-Júnior G; de Mello MP
    Sex Dev; 2017; 11(1):34-39. PubMed ID: 28081536
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.